Effects of Biofeedback-Guided Training on Muscle Strength and Postural Alignment in Upper Cross Syndrome.
1 other identifier
interventional
56
1 country
1
Brief Summary
This randomized controlled trial investigates the effects of biofeedback-guided training versus conventional therapy on muscle strength and postural alignment in patients with Upper Cross Syndrome. The study includes adults aged 25-45 years meeting diagnostic criteria for UCS, such as weak deep cervical flexors, restricted cervical ROM, forward head posture, increased thoracic kyphosis, and chronic neck pain \>3 months. Participants are divided into two groups: Group A biofeedback training and Group B conventional therapy, receiving 12 sessions over 4 weeks ,3sessions/week. Assessments are conducted at baseline, post-1st session, and weekly intervals using standardized measures.The study aims to compare the efficacy of biofeedback-guided training in improving strength and posture in UCS patients.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Aug 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 11, 2025
CompletedFirst Posted
Study publicly available on registry
June 18, 2025
CompletedStudy Start
First participant enrolled
August 11, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2026
CompletedAugust 22, 2025
August 1, 2025
5 months
June 11, 2025
August 18, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
cranio-cervical flexion test
craniocervical flexion test to measure strength and endurance of Deep cervical flexors. it ranges from 20 mm of hg to 30 mm of Hg based on increased strength
baseline to 4th week
Secondary Outcomes (8)
NPRS
total of 5 measurements taken at baseline, at the end of 1st, 2nd , 3rd and 4th week
NECK DISABILITY INDEX
total of 5 measurements taken at baseline, at the end of 1st, 2nd , 3rd and 4th week
cervical Flexion
baseline to 4th week
cervical Extension
baseline to 4th week
cervical Rt rotation
baseline to 4th week
- +3 more secondary outcomes
Study Arms (2)
Experimental Group
EXPERIMENTALBiofeedback-Guided Strength Training: Hot Pack: Applied for 10 minutes, mild warmth sensation to relax muscles and prepare for exercise. 1\. BPU (Biofeedback Pressure Unit): performed at 5 pressure levels (22, 24, 26, 28, 30 mmHg). Each level involves a 10-second hold, with 30 seconds rest between levels. Targeted muscles: * Deep Cervical Flexors (Capitus Longus, Capitus Colli). * Rhomboids * Trapezius Total duration (BPU): 20 minutes/session, performed 3 times/week.
Control Group
ACTIVE COMPARATORConventional Therapy: Hot Pack: Applied for 10 minutes, mild warmth sensation to relax muscles and prepare for exercise. EXERCISE PROGRAM: * 1\. Supine: Neck curl with Chin Tucks (Deep Cervical Flexors Capitus Longus, Capitus Colli): 10 reps/session, holding each for 5 seconds. * 2\. Sitting: Chin tuck with Head pushing against palm. * 3\. Chin Up (Middle and Lower Trapezius): 10 reps/session, holding each for 5 seconds. * 4\. Scapular Squeezes (Rhomboids): 2-3 sets of 10 reps/session, holding each for 5 seconds * 5\. Doorway Pectoral Stretch (pect major) 2-3 reps, 30 sec hold (36) Total duration: 20 minutes/session, performed 3 times/week.
Interventions
Hot Pack: Applied for 10 minutes, mild warmth sensation to relax muscles and prepare for exercise. 1\. BPU (Biofeedback Pressure Unit): performed at 5 pressure levels (22, 24, 26, 28, 30 mmHg). Each level involves a 10-second hold, with 30 seconds rest between levels. Targeted muscles: * Deep Cervical Flexors (Capitus Longus, Capitus Colli). * Rhomboids * Trapezius Total duration (BPU): 20 minutes/session, performed 3 times/week.
Hot Pack: Applied for 10 minutes, mild warmth sensation to relax muscles and prepare for exercise. EXERCISE PROGRAM: * 1\. Supine: Neck curl with Chin Tucks (Deep Cervical Flexors Capitus Longus, Capitus Colli): 10 reps/session, holding each for 5 seconds. * 2\. Sitting: Chin tuck with Head pushing against palm. * 3\. Chin Up (Middle and Lower Trapezius): 10 reps/session, holding each for 5 seconds. * 4\. Scapular Squeezes (Rhomboids): 2-3 sets of 10 reps/session, holding each for 5 seconds• 5. Doorway Pectoral Stretch (pect major) 2-3 reps, 30 sec hold (36)Total duration: 20 minutes/session, performed 3 times/week.
Eligibility Criteria
You may qualify if:
- Adults aged 25-45 years with both genders.
- Individuals meeting the following diagnostic criteria for upper cross syndrome will be included:
- Reduced strength of deep cervical flexors = unable to maintain pressure beyond 22-24 mm Hg (assessed via cranio-cervical flexion test).
- Limited cervical range of motion (Flexion: \< 80 degrees, Extension: \< 70 degrees, Rotation: \< 90 degrees on both sides, Lateral Flexion: \< 20 degrees)
- Postural deviations: forward head posture (CVA \<50 degrees), increased thoracic kyphosis (via flexi curve \>45 degrees).
- Neck pain with a duration of over 3 months
You may not qualify if:
- History of recent neck surgery or injury.
- Patients with neurological disorders affecting muscle tone.
- Involvement in other physical therapy programs focused on UCS.
- Diagnosed musculoskeletal condition that could impact muscle performance.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Watch Guard Tech
Rawalpindi, Punjab Province, 46000, Pakistan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Aisha Razzaq, PHD*
Riphah International University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, INVESTIGATOR
- Masking Details
- Participants will be masked by using sealed envolpe method
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 11, 2025
First Posted
June 18, 2025
Study Start
August 11, 2025
Primary Completion
January 1, 2026
Study Completion
January 1, 2026
Last Updated
August 22, 2025
Record last verified: 2025-08
Data Sharing
- IPD Sharing
- Will not share